Clinical Trials Site Coordinator | Meaningful Impact

Medex Smo; Selçuklu; On-site; TRY 167,400 - 256,680; Full time

Benefits offered by this job

Certification opportunities

Workshops in clinical research

Job summary

Medex Smo is seeking a Site Coordinator to oversee clinical trial activities under the Principal Investigator. The role includes planning daily tasks, ensuring protocol compliance, and safeguarding participant safety.

You will facilitate sponsor communications and data collection while maintaining regulatory oversight. Responsibilities include assisting in volunteer screening, organizing visits, and ensuring proper documentation.

Qualifications

• Bachelor's degree minimum.
• Understanding of regulatory requirements and GCP guidelines.
• At least intermediate level English.
• Ability to manage time effectively and handle multiple tasks.

Responsibilities

• Coordinate trial activities under the supervision of the Principal Investigator.
• Assist in screening volunteers and organizing visits.
• Maintain study documentation and regulatory files.
• Ensure timely collection and handling of laboratory samples.
• Report and document adverse events as per protocol.

Skills

Regulatory knowledge

GCP guidelines

Time management

Ethical handling

Intermediate English

Education

Bachelor's degree

Master/PhD preferred

Job description

Medex Smo is seeking a Site Coordinator to oversee clinical trial activities under the Principal Investigator. The role includes planning daily tasks, ensuring protocol compliance, and safeguarding participant safety.

You will facilitate sponsor communications and data collection while maintaining regulatory oversight. Responsibilities include assisting in volunteer screening, organizing visits, and ensuring proper documentation.